US8124630B2
(en)
|
1999-01-13 |
2012-02-28 |
Bayer Healthcare Llc |
ω-carboxyaryl substituted diphenyl ureas as raf kinase inhibitors
|
CA2359244C
(en)
|
1999-01-13 |
2013-10-08 |
Bayer Corporation |
.omega.-carboxy aryl substituted diphenyl ureas as p38 kinase inhibitors
|
AU2003209119A1
(en)
|
2002-02-11 |
2003-09-04 |
Bayer Pharmaceuticals Corporation |
Pyridine, quinoline, and isoquinoline n-oxides as kinase inhibitors
|
MXPA04007832A
(en)
|
2002-02-11 |
2005-09-08 |
Bayer Pharmaceuticals Corp |
Aryl ureas with angiogenesis inhibiting activity.
|
MXPA04009541A
(en)
*
|
2002-03-29 |
2005-01-25 |
Chiron Corp |
Substituted benzazoles and use thereof as raf kinase inhibitors.
|
US8299108B2
(en)
*
|
2002-03-29 |
2012-10-30 |
Novartis Ag |
Substituted benzazoles and methods of their use as inhibitors of raf kinase
|
DE10224892A1
(en)
*
|
2002-06-04 |
2003-12-18 |
Aventis Pharma Gmbh |
Substituted thiophenes, process for their preparation, their use as a medicament or diagnostic agent, and medicament containing them
|
US7531553B2
(en)
*
|
2003-03-21 |
2009-05-12 |
Amgen Inc. |
Heterocyclic compounds and methods of use
|
WO2004087153A2
(en)
*
|
2003-03-28 |
2004-10-14 |
Chiron Corporation |
Use of organic compounds for immunopotentiation
|
MXPA05012377A
(en)
|
2003-05-15 |
2006-05-25 |
Arqule Inc |
Imidazothiazoles and imidazoxazole derivatives as inhibitors of p38.
|
DE602004007382T2
(en)
|
2003-05-20 |
2008-04-17 |
Bayer Pharmaceuticals Corp., West Haven |
DIARYL UREAS FOR PDGFR MEDIATED DISEASES
|
DE10344223A1
(en)
*
|
2003-09-24 |
2005-04-21 |
Merck Patent Gmbh |
New 2-anilino-1,3-benzoxazole derivatives, are inhibitors of kinases, especially tyrosine- or Raf-kinases, useful e.g. for treating solid tumors, angiogenesis, diabetic retinopathy, inflammation or psoriasis
|
JP4755991B2
(en)
*
|
2003-10-16 |
2011-08-24 |
ノバルティス バクシンズ アンド ダイアグノスティックス,インコーポレーテッド |
Substituted benzazoles and their use as Raf kinase inhibitors
|
DE10349587A1
(en)
*
|
2003-10-24 |
2005-05-25 |
Merck Patent Gmbh |
Benzimidazolylderivate
|
US7772234B2
(en)
*
|
2003-11-19 |
2010-08-10 |
Array Biopharma Inc. |
Bicyclic inhibitors of MEK and methods of use thereof
|
US7470712B2
(en)
*
|
2004-01-21 |
2008-12-30 |
Bristol-Myers Squibb Company |
Amino-benzazoles as P2Y1 receptor inhibitors
|
GB0401334D0
(en)
*
|
2004-01-21 |
2004-02-25 |
Novartis Ag |
Organic compounds
|
BRPI0507373A
(en)
|
2004-01-23 |
2007-07-10 |
Amgen Inc |
compounds and method of use
|
AU2005207946A1
(en)
|
2004-01-23 |
2005-08-11 |
Amgen Inc. |
Quinoline quinazoline pyridine and pyrimidine counds and their use in the treatment of inflammation angiogenesis and cancer
|
TW200530236A
(en)
|
2004-02-23 |
2005-09-16 |
Chugai Pharmaceutical Co Ltd |
Heteroaryl phenylurea
|
WO2005118543A1
(en)
*
|
2004-06-03 |
2005-12-15 |
Ono Pharmaceutical Co., Ltd. |
Kinase inhibitor and use thereof
|
EP1761506A1
(en)
*
|
2004-06-15 |
2007-03-14 |
AstraZeneca AB |
Substituted quinazolones as anti-cancer agents
|
TW200616974A
(en)
*
|
2004-07-01 |
2006-06-01 |
Astrazeneca Ab |
Chemical compounds
|
US7829560B2
(en)
*
|
2004-07-08 |
2010-11-09 |
Arqule, Inc. |
1,4-disubstituted naphthalenes as inhibitors of P38 MAP kinase
|
CA2578283A1
(en)
*
|
2004-08-25 |
2006-03-02 |
Targegen, Inc. |
Heterocyclic compounds and methods of use
|
CN101048388A
(en)
*
|
2004-08-31 |
2007-10-03 |
阿斯利康(瑞典)有限公司 |
Quinazolinone derivatives and their use as B-Raf inhibitors
|
KR20070055575A
(en)
*
|
2004-09-01 |
2007-05-30 |
아스트라제네카 아베 |
Quinazolinone derivatives and their use as b-raf inhibitors
|
WO2006040568A1
(en)
*
|
2004-10-15 |
2006-04-20 |
Astrazeneca Ab |
Quinoxalines as b raf inhibitors
|
EP1809636A1
(en)
*
|
2004-10-19 |
2007-07-25 |
Arqule, Inc. |
Synthesis of imidazooxazole and imidazothiazole inhibitors of p38 map kinase
|
CN101068592B
(en)
*
|
2004-11-05 |
2010-12-08 |
Icu医疗公司 |
Medical connector with the property of high flow rate
|
EP1827434B1
(en)
|
2004-11-30 |
2014-01-15 |
Amgen Inc. |
Quinolines and quinazoline analogs and their use as medicaments for treating cancer
|
CA2589773A1
(en)
*
|
2004-12-22 |
2006-06-29 |
Astrazeneca Ab |
Pyridine carboxamide derivatives for use as anticancer agents
|
EP1674466A1
(en)
*
|
2004-12-27 |
2006-06-28 |
4Sc Ag |
2,5- and 2,6-disubstituted benzazole analogues useful as protein kinase inhibitors
|
US7576090B2
(en)
*
|
2004-12-27 |
2009-08-18 |
4Sc Ag |
Benzazole analogues and uses thereof
|
US7429608B2
(en)
*
|
2005-01-20 |
2008-09-30 |
Amgen Inc. |
Benzo[d]imidazol analogs as vanilloid receptor ligands and their use in treatments
|
AU2006208834A1
(en)
*
|
2005-01-25 |
2006-08-03 |
Astrazeneca Ab |
Chemical compounds
|
NZ580974A
(en)
|
2005-02-18 |
2011-05-27 |
Novartis Vaccines & Diagnostic |
Immunogens from uropathogenic escherichia coli
|
HUE027400T2
(en)
|
2005-02-18 |
2016-10-28 |
Glaxosmithkline Biologicals Sa |
Proteins and nucleic acids from meningitis/sepsis-associated escherichia coli
|
JO2787B1
(en)
|
2005-04-27 |
2014-03-15 |
امجين إنك, |
Substituted Amid derivatives & methods of use
|
TWI370820B
(en)
|
2005-04-27 |
2012-08-21 |
Takeda Pharmaceutical |
Fused heterocyclic compounds
|
WO2006124780A2
(en)
*
|
2005-05-12 |
2006-11-23 |
Kalypsys, Inc. |
Ih-benzo [d] imidazole compounds as inhibitors of b-raf kinase
|
EP2614709A1
(en)
|
2005-07-18 |
2013-07-17 |
Novartis AG |
Small animal model for HCV replication
|
CN101253169B
(en)
*
|
2005-08-30 |
2011-11-23 |
诺瓦提斯公司 |
Substituted benzimidazoles and methods of preparation
|
PE20070427A1
(en)
*
|
2005-08-30 |
2007-04-21 |
Novartis Ag |
BENZIMIDAZOLES DERIVED COMPOUNDS SUBSTITUTED AS TYROSINE KINASE INHIBITORS
|
CN101331120A
(en)
|
2005-10-13 |
2008-12-24 |
史密丝克莱恩比彻姆公司 |
Novel heterocycle compounds
|
AU2006310336B2
(en)
|
2005-11-04 |
2011-02-03 |
Seqirus UK Limited |
Adjuvanted vaccines with non-virion antigens prepared from influenza viruses grown in cell culture
|
EP1951302A2
(en)
|
2005-11-04 |
2008-08-06 |
Novartis Vaccines and Diagnostics S.r.l. |
Influenza vaccine with reduced amount of oil-in-water emulsion as adjuvant
|
AU2006310337B9
(en)
|
2005-11-04 |
2013-11-28 |
Novartis Ag |
Adjuvanted influenza vaccines including cytokine-inducing agents
|
CA2628328A1
(en)
|
2005-11-04 |
2007-05-10 |
Novartis Vaccines And Diagnostics S.R.L. |
Influenza vaccines including combinations of particulate adjuvants and immunopotentiators
|
EP1966159A2
(en)
*
|
2005-12-22 |
2008-09-10 |
AstraZeneca AB |
Chemical compounds
|
US20070155746A1
(en)
*
|
2005-12-23 |
2007-07-05 |
Kalypsys, Inc. |
Novel substituted pyridinyloxy and pyrimidinyloxy amides useful as inhibitors of protein kinases
|
JO2660B1
(en)
|
2006-01-20 |
2012-06-17 |
نوفارتيس ايه جي |
PI-3 Kinase inhibitors and methods of their use
|
EA015271B1
(en)
|
2006-01-27 |
2011-06-30 |
Новартис Вэксинс Энд Диагностикс Гмбх & Ко Кг |
Influenza vaccines containing hemagglutinin and matrix proteins
|
JP5133071B2
(en)
|
2006-02-09 |
2013-01-30 |
第一三共株式会社 |
Anticancer pharmaceutical composition
|
AU2007215247B2
(en)
|
2006-02-10 |
2012-12-13 |
Transtech Pharma, Llc |
Benzazole derivatives, compositions, and methods of use as Aurora kinase inhibitors
|
AU2007227681A1
(en)
|
2006-03-15 |
2007-09-27 |
Wyeth |
N-substituted-azacyclylamines as histamine-3 antagonists
|
ES2536426T3
(en)
|
2006-03-23 |
2015-05-25 |
Novartis Ag |
Imidazoquinoxaline compounds as immunomodulators
|
EP2382987A1
(en)
|
2006-03-24 |
2011-11-02 |
Novartis Vaccines and Diagnostics GmbH |
Storage of influenza vaccines without refrigeration
|
EP2382988A1
(en)
|
2006-03-31 |
2011-11-02 |
Novartis AG |
Combined mucosal and parenteral immunization against HIV
|
AR060358A1
(en)
|
2006-04-06 |
2008-06-11 |
Novartis Vaccines & Diagnostic |
QUINAZOLINS FOR THE INHIBITION OF PDK 1
|
LT2010528T
(en)
|
2006-04-19 |
2017-12-27 |
Novartis Ag |
6-o-substituted benzoxazole and benzothiazole compounds and methods of inhibiting csf-1r signaling
|
CA2649913A1
(en)
*
|
2006-05-19 |
2007-11-29 |
Wyeth |
N-benzoyl- and n-benzylpyrrolidin-3-ylamines as histamine-3 antagonists
|
PT2054431E
(en)
|
2006-06-09 |
2011-11-03 |
Novartis Ag |
Conformers of bacterial adhesins
|
US7932390B2
(en)
*
|
2006-06-29 |
2011-04-26 |
Hoffman-La Roche Inc. |
Substituted thieno[3,2-C]pyridine carboxylic acid derivatives
|
GB0614460D0
(en)
|
2006-07-20 |
2006-08-30 |
Novartis Ag |
Vaccines
|
PT2046292E
(en)
*
|
2006-07-21 |
2010-04-26 |
Novartis Ag |
Formulations for benzimidazolyl pyridyl ethers
|
US20100166788A1
(en)
|
2006-08-16 |
2010-07-01 |
Novartis Vaccines And Diagnostics |
Immunogens from uropathogenic escherichia coli
|
PE20130814A1
(en)
|
2006-08-30 |
2013-08-08 |
Novartis Ag |
BENZIMIDAZOLYL PYRIDYL ETHER SALTS AND FORMULATIONS CONTAINING THEM
|
NZ575410A
(en)
*
|
2006-09-07 |
2012-03-30 |
Biogen Idec Inc |
2-(1H-Indazol-3-ylamino)-1H-benzimidazole derivatives
|
EA200970271A1
(en)
|
2006-09-11 |
2010-02-26 |
Новартис Аг |
OBTAINING VACCINES AGAINST THE VIRUS OF THE INFLUENZA WITHOUT USING THE CHICKEN EMBRYOS
|
PE20081152A1
(en)
|
2006-10-06 |
2008-08-10 |
Wyeth Corp |
N-SUBSTITUTED AZACYCLYLAMINES AS HISTAMINE-3 ANTAGONISTS
|
WO2008068631A2
(en)
|
2006-12-06 |
2008-06-12 |
Novartis Ag |
Vaccines including antigen from four strains of influenza virus
|
GB0700562D0
(en)
|
2007-01-11 |
2007-02-21 |
Novartis Vaccines & Diagnostic |
Modified Saccharides
|
US8324389B2
(en)
*
|
2007-03-02 |
2012-12-04 |
Novartis Ag |
Solid forms of a Raf kinase inhibitor
|
CN101754965B
(en)
*
|
2007-05-21 |
2014-03-19 |
诺华股份有限公司 |
CSF-1R inhibitors, compositions, and methods of use
|
JP5352476B2
(en)
*
|
2007-06-05 |
2013-11-27 |
武田薬品工業株式会社 |
Bicyclic heterocyclic compounds as kinase inhibitors
|
BRPI0813866A2
(en)
|
2007-06-27 |
2015-01-06 |
Novartis Ag |
VACCINES AGAINST INFLUENCE WITH LOW ADDITIVE CONTENT
|
CL2008002088A1
(en)
|
2007-07-16 |
2008-09-05 |
Wyeth Corp |
COMPOUNDS DERIVED FROM REPLACED PHENYLL, HISTAMINE RECEIVER MODULATORS 3; PREPARATION PROCESS; PHARMACEUTICAL COMPOSITION; AND USE IN THE TREATMENT OF COGNITIVE DISORDERS SUCH AS DEMENTIA, ALZHEIMER, AMONG OTHERS.
|
GB0713880D0
(en)
|
2007-07-17 |
2007-08-29 |
Novartis Ag |
Conjugate purification
|
GB0714963D0
(en)
|
2007-08-01 |
2007-09-12 |
Novartis Ag |
Compositions comprising antigens
|
MX2010001636A
(en)
|
2007-08-14 |
2010-03-15 |
Hoffmann La Roche |
Diazo bicyclic smac mimetics and the uses thereof.
|
US8324395B2
(en)
|
2007-08-23 |
2012-12-04 |
Takeda Pharmaceutical Company Limited |
Heterocyclic compound and use thereof
|
EP2184285B1
(en)
*
|
2007-08-29 |
2015-11-04 |
Takeda Pharmaceutical Company Limited |
Heterocyclic compound and use thereof
|
WO2009028655A1
(en)
*
|
2007-08-30 |
2009-03-05 |
Takeda Pharmaceutical Company Limited |
Heterocyclic compound and use thereof
|
AU2008305294B2
(en)
|
2007-09-21 |
2012-11-29 |
Array Biopharma Inc. |
Pyridin-2 -yl-amino-1, 2, 4 -thiadiazole derivatives as glucokinase activators for the treatment of diabetes mellitus
|
US20100261679A1
(en)
*
|
2007-10-18 |
2010-10-14 |
James Sutton |
CSF-1R, Inhibitors, Compositions, and Methods of Use
|
WO2009058267A2
(en)
*
|
2007-10-29 |
2009-05-07 |
Amgen Inc. |
Benzomorpholine derivatives and methods of use
|
GB0810305D0
(en)
|
2008-06-05 |
2008-07-09 |
Novartis Ag |
Influenza vaccination
|
JP2011506560A
(en)
|
2007-12-20 |
2011-03-03 |
ノバルティス アーゲー |
Thiazole derivatives used as PI3 kinase inhibitors
|
GB0818453D0
(en)
|
2008-10-08 |
2008-11-12 |
Novartis Ag |
Fermentation processes for cultivating streptococci and purification processes for obtaining cps therefrom
|
WO2009111280A1
(en)
*
|
2008-02-29 |
2009-09-11 |
Array Biopharma Inc. |
N- (6-aminopyridin-3-yl) -3- (sulfonamido) benzamide derivatives as b-raf inhibitors for the treatment of cancer
|
PE20091623A1
(en)
*
|
2008-02-29 |
2009-11-19 |
Array Biopharma Inc |
1H-PYRAZOLO [3,4-b] PYRIDINE DERIVATIVES AS RAF KINASE INHIBITORS
|
CA2716947A1
(en)
*
|
2008-02-29 |
2009-09-11 |
Array Biopharma Inc. |
Imidazo [4,5-b] pyridine derivatives used as raf inhibitors
|
AR070535A1
(en)
*
|
2008-02-29 |
2010-04-14 |
Array Biopharma Inc |
RAF INHIBITING COMPOUNDS AND METHODS FOR USE
|
KR20100135766A
(en)
|
2008-03-18 |
2010-12-27 |
노파르티스 아게 |
Improvements in preparation of influenza virus vaccine antigens
|
US20110092546A1
(en)
*
|
2008-06-13 |
2011-04-21 |
Novartis Ag |
Substituted benzimidazoles for neurofibromatosis
|
UY32138A
(en)
|
2008-09-25 |
2010-04-30 |
Boehringer Ingelheim Int |
SUBSTITUTED AMIDES 2- (2,6-DICLORO-PHENYLAMINE) -6-FLUORO-1-METHYL-1H-BENCIMIDAZOL-5-CARBOXYL AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS
|
JP5579619B2
(en)
|
2008-12-01 |
2014-08-27 |
武田薬品工業株式会社 |
Heterocyclic compounds and uses thereof
|
JO3101B1
(en)
|
2008-12-02 |
2017-09-20 |
Takeda Pharmaceuticals Co |
Benzothiazole derivatives as anticancer agents
|
WO2010065893A1
(en)
*
|
2008-12-05 |
2010-06-10 |
Arqule, Inc. |
Raf inhibitors and their uses
|
US8585505B2
(en)
|
2008-12-15 |
2013-11-19 |
Tetris Online, Inc. |
Inter-game interactive hybrid asynchronous computer game infrastructure
|
SI2391366T1
(en)
*
|
2009-01-29 |
2013-01-31 |
Novartis Ag |
Substituted benzimidazoles for the treatment of astrocytomas
|
UY32470A
(en)
|
2009-03-05 |
2010-10-29 |
Boehringer Ingelheim Int |
DERIVATIVES OF 2- {2-CHLORINE-5 - [(REPLACED) METHYL] PHENYLAMINE} -1-METHYL] PHENYLAMINE} -1-METHYLBENCIMIDAZOL-5-CARBOXAMIDES-N- (SUBSTITUTED) AND ITS PHYSIOLOGICALLY ACCEPTABLE SALTS, COMPOSITIONS AND APPLIANCE
|
RU2011140508A
(en)
|
2009-03-06 |
2013-04-20 |
Новартис Аг |
Chlamydia antigens
|
PL2510947T3
(en)
|
2009-04-14 |
2016-09-30 |
|
Compositions for immunising against Staphylococcus aureus
|
BE1019643A3
(en)
|
2009-04-27 |
2012-09-04 |
Novartis Ag |
INFLUENZA PROTECTION VACCINES.
|
EP2445345B1
(en)
|
2009-06-23 |
2014-08-27 |
The Translational Genomics Research Institute |
Benzamide derivatives
|
US8293753B2
(en)
|
2009-07-02 |
2012-10-23 |
Novartis Ag |
Substituted 2-carboxamide cycloamino ureas
|
AU2010269961A1
(en)
|
2009-07-07 |
2012-02-02 |
Novartis Ag |
Conserved Escherichia coli immunogens
|
BR112012001666A2
(en)
|
2009-07-15 |
2019-09-24 |
Novartis Ag |
rsv f protein compositions and methods for making the same
|
ES2526996T3
(en)
|
2009-07-16 |
2015-01-19 |
Novartis Ag |
Detoxified immunogens from Escherichia coli
|
GB0918392D0
(en)
|
2009-10-20 |
2009-12-02 |
Novartis Ag |
Diagnostic and therapeutic methods
|
GB0919690D0
(en)
|
2009-11-10 |
2009-12-23 |
Guy S And St Thomas S Nhs Foun |
compositions for immunising against staphylococcus aureus
|
ES2707778T3
(en)
|
2009-12-30 |
2019-04-05 |
Glaxosmithkline Biologicals Sa |
Immunogens polysaccharides conjugated with carrier proteins of E. coli
|
GB201009861D0
(en)
|
2010-06-11 |
2010-07-21 |
Novartis Ag |
OMV vaccines
|
US9192661B2
(en)
|
2010-07-06 |
2015-11-24 |
Novartis Ag |
Delivery of self-replicating RNA using biodegradable polymer particles
|
US9120752B2
(en)
|
2010-07-16 |
2015-09-01 |
Purdue Pharma, L.P. |
Pyridine compounds as sodium channel blockers
|
AR082418A1
(en)
|
2010-08-02 |
2012-12-05 |
Novartis Ag |
CRYSTAL FORMS OF 1- (4-METHYL-5- [2- (2,2,2-TRIFLUORO-1,1-DIMETHYL-Ethyl) -PIRIDIN-4-IL] -TIAZOL-2-IL) -AMIDE OF 2 -AMIDA OF THE ACID (S) -PIRROLIDIN-1,2-DICARBOXILICO
|
US8586604B2
(en)
|
2010-08-20 |
2013-11-19 |
Boehringer Ingelheim International Gmbh |
Inhibitors of the microsomal prostaglandin E2 synthase-1
|
US8759537B2
(en)
|
2010-08-20 |
2014-06-24 |
Boehringer Ingelheim International Gmbh |
3H-imidazo [4, 5-C] pyridine-6-carboxamides as anti-inflammatory agents
|
AU2011303597A1
(en)
|
2010-09-17 |
2013-04-11 |
Purdue Pharma L.P. |
Pyridine compounds and the uses thereof
|
RU2017135541A
(en)
*
|
2010-11-19 |
2019-02-08 |
Лиганд Фармасьютикалс Инкорпорейтед |
HETEROCYCLIC AMINES AND THEIR APPLICATIONS
|
US8466186B2
(en)
|
2010-12-10 |
2013-06-18 |
Boehringer Ingelheim International Gmbh |
Compounds
|
UY33779A
(en)
|
2010-12-10 |
2012-07-31 |
Boehringer Ingelheim Int |
? 2- (Phenylamino) -1H-benzimidazol-5-carboxamides novel?
|
US8486968B2
(en)
|
2010-12-10 |
2013-07-16 |
Boehringer Ingelheim International Gmbh |
Compounds
|
US10342862B2
(en)
|
2011-01-26 |
2019-07-09 |
Glaxosmithkline Biologicals, Sa |
RSV immunization regimen
|
AP2013007043A0
(en)
|
2011-01-31 |
2013-08-31 |
Novartis Ag |
Novel heterocyclic derivatives
|
JP2014519819A
(en)
|
2011-05-13 |
2014-08-21 |
ノバルティス アーゲー |
RSVF antigen before fusion
|
JP6088507B2
(en)
|
2011-07-08 |
2017-03-01 |
ノバルティス アーゲー |
Tyrosine ligation method
|
CN102432595B
(en)
*
|
2011-09-14 |
2013-09-25 |
湖南有色凯铂生物药业有限公司 |
N-indole-1-amides compounds and application of N-indole-1-amides compounds as anti-cancer drugs
|
JP6059731B2
(en)
|
2011-10-28 |
2017-01-11 |
ノバルティス アーゲー |
Novel purine derivatives and their use in the treatment of diseases
|
EP2776069A1
(en)
|
2011-11-07 |
2014-09-17 |
Novartis AG |
Carrier molecule comprising a spr0096 and a spr2021 antigen
|
WO2013108272A2
(en)
|
2012-01-20 |
2013-07-25 |
International Centre For Genetic Engineering And Biotechnology |
Blood stage malaria vaccine
|
WO2013136170A1
(en)
|
2012-03-16 |
2013-09-19 |
Purdue Pharma L.P. |
Substituted pyridines as sodium channel blockers
|
CA2872526A1
(en)
|
2012-05-16 |
2013-11-21 |
Novartis Ag |
Dosage regimen for a pi-3 kinase inhibitor
|
BR112015007126A2
(en)
|
2012-10-02 |
2017-08-08 |
Glaxosmithkline Biologicals Sa |
composition, method for inducing an immune response, and use of a composition
|
SG11201504258RA
(en)
|
2012-11-30 |
2015-07-30 |
Glaxosmithkline Biolog Sa |
Pseudomonas antigens and antigen combinations
|
WO2014096941A1
(en)
|
2012-12-20 |
2014-06-26 |
Purdue Pharma L.P. |
Cyclic sulfonamides as sodium channel blockers
|
US9242969B2
(en)
|
2013-03-14 |
2016-01-26 |
Novartis Ag |
Biaryl amide compounds as kinase inhibitors
|
US9556170B2
(en)
|
2013-08-30 |
2017-01-31 |
University Of Utah Research Foundation |
Substituted-1H-benzo[d]imidazole series compounds as lysine-specific demethylase 1 (LSD1) inhibitors
|
CN103450093A
(en)
*
|
2013-09-06 |
2013-12-18 |
中国药科大学 |
2-aminobenzimidazoles and applications thereof
|
WO2015041533A1
(en)
|
2013-09-20 |
2015-03-26 |
Stichting Het Nederlands Kanker Instituut |
Rock in combination with mapk-pathway
|
WO2015041534A1
(en)
|
2013-09-20 |
2015-03-26 |
Stichting Het Nederlands Kanker Instituut |
P90rsk in combination with raf/erk/mek
|
EP2870974A1
(en)
|
2013-11-08 |
2015-05-13 |
Novartis AG |
Salmonella conjugate vaccines
|
US20170000778A1
(en)
|
2013-12-06 |
2017-01-05 |
Emmanuelle di Tomaso |
Dosage regimen for an alpha-isoform selective phosphatidylinositol 3-kinase inhibitor
|
CA2935683A1
(en)
*
|
2013-12-30 |
2015-07-09 |
Lifesci Pharmaceuticals, Inc. |
Therapeutic inhibitory compounds
|
US10730866B2
(en)
|
2014-04-07 |
2020-08-04 |
Purdue Pharma L.P. |
Indole derivatives and use thereof
|
WO2015156674A2
(en)
|
2014-04-10 |
2015-10-15 |
Stichting Het Nederlands Kanker Instituut |
Method for treating cancer
|
WO2015178770A1
(en)
|
2014-05-19 |
2015-11-26 |
Stichting Het Nederlands Kanker Instituut |
Compositions for cancer treatment
|
UY36294A
(en)
|
2014-09-12 |
2016-04-29 |
Novartis Ag |
COMPOUNDS AND COMPOSITIONS AS QUINASA INHIBITORS
|
WO2016100184A1
(en)
|
2014-12-16 |
2016-06-23 |
Forum Pharmaceuticals, Inc. |
Geminal substituted quinuclidine amide compounds as agonists of alpha-7 nicotinic acetylcholine receptors
|
CN105949178B
(en)
*
|
2015-03-09 |
2020-05-26 |
西格莱(苏州)生物医药有限公司 |
Benzimidazole compound, preparation method, intermediate and application thereof
|
US10807983B2
(en)
|
2015-03-16 |
2020-10-20 |
Ligand Pharmaceuticals, Inc. |
Imidazo-fused heterocycles and uses thereof
|
KR20180044256A
(en)
|
2015-06-10 |
2018-05-02 |
엑소반트 사이언시즈 게엠베하 |
Aminobenzoisooxazole compounds as agonists of the A7-nicotinic acetylcholine receptor
|
US10428062B2
(en)
|
2015-08-12 |
2019-10-01 |
Axovant Sciences Gmbh |
Geminal substituted aminobenzisoxazole compounds as agonists of α7-nicotinic acetylcholine receptors
|
KR101770310B1
(en)
|
2015-08-24 |
2017-08-24 |
이화여자대학교 산학협력단 |
2-(phenylamino)benzo[d]oxazol-5-ol derivatives, preparation method thereof, and pharmaceutical composition for use in preventing or treating inflammatory diseases containing the same as an active ingredient
|
JP2018532750A
(en)
|
2015-11-02 |
2018-11-08 |
ノバルティス アーゲー |
Dosage regimen of phosphatidylinositol 3-kinase inhibitor
|
WO2018060833A1
(en)
|
2016-09-27 |
2018-04-05 |
Novartis Ag |
Dosage regimen for alpha-isoform selective phosphatidylinositol 3-kinase inhibitor alpelisib
|
WO2018168899A1
(en)
*
|
2017-03-15 |
2018-09-20 |
大日本住友製薬株式会社 |
Method for producing benzimidazole derivative
|
JP2022500385A
(en)
|
2018-09-10 |
2022-01-04 |
ミラティ セラピューティクス, インコーポレイテッド |
Combination therapy
|
US20230183204A9
(en)
*
|
2018-11-07 |
2023-06-15 |
Dana-Farber Cancer Institute, Inc. |
Benzimidazole derivatives and aza-benzimidazole derivatives as janus kinase 2 inhibitors and uses thereof
|
CN111848505A
(en)
*
|
2019-04-26 |
2020-10-30 |
广东东阳光药业有限公司 |
Preparation method of vatacostat intermediate
|
KR102337399B1
(en)
*
|
2019-10-02 |
2021-12-09 |
주식회사 클로소사이언스 |
Compounds that induces anti-aging gene klotho and use thereof
|
CN111138428B
(en)
*
|
2019-12-26 |
2021-02-19 |
深圳市老年医学研究所 |
Preparation method of African tetrandrine and African tetrandrine
|
TW202204350A
(en)
|
2020-05-06 |
2022-02-01 |
美商雅捷可斯治療公司 |
6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors
|
JP2023554392A
(en)
*
|
2020-12-16 |
2023-12-27 |
アイエフエム デュー インコーポレイテッド |
Compounds and compositions for treating conditions associated with STING activity
|
JP2024505537A
(en)
*
|
2021-01-29 |
2024-02-06 |
コリア リサーチ インスティチュート オブ ケミカル テクノロジー |
Benzothiazole and benzimidazole derivatives, pharmaceutically acceptable salts, processes for their production, and pharmaceutical compositions containing them as active ingredients
|
US20230167110A1
(en)
*
|
2021-11-09 |
2023-06-01 |
Ajax Therapeutics, Inc. |
6-heteroaryloxy benzimidazoles and azabenzimidazoles as jak2 inhibitors
|